Morphology and Microstructure Evolution of Gold Nanostructures in the Limited Volume Porous Matrices

The modern development of nanotechnology requires the discovery of simple approaches that ensure the controlled formation of functional nanostructures with a predetermined morphology. One of the simplest approaches is the self-assembly of nanostructures. The widespread implementation of self-assembly is limited by the complexity of controlled processes in a large volume where, due to the temperature, ion concentration, and other thermodynamics factors, local changes in diffusion-limited processes may occur, leading to unexpected nanostructure growth. The easiest ways to control the diffusion-limited processes are spatial limitation and localized growth of nanostructures in a porous matrix. In this paper, we propose to apply the method of controlled self-assembly of gold nanostructures in a limited pore volume of a silicon oxide matrix with submicron pore sizes. A detailed study of achieved gold nanostructures' morphology, microstructure, and surface composition at different formation stages is carried out to understand the peculiarities of realized nanostructures. Based on the obtained results, a mechanism for the growth of gold nanostructures in a limited volume, which can be used for the controlled formation of nanostructures with a predetermined geometry and composition, has been proposed. The results observed in the present study can be useful for the design of plasmonic-active surfaces for surface-enhanced Raman spectroscopy-based detection of ultra-low concentration of different chemical or biological analytes, where the size of the localized gold nanostructures is comparable with the spot area of the focused laser beam

Synthesis, Phase Transformations and Strength Properties of Nanostructured (1 − x)ZrO2 − xCeO2 Composite Ceramics

The aim of this work is to study the properties of nanostructured (1 − x)ZrO2 − xCeO2 composite ceramics, depending on the content of oxide components, as well as to establish the relationship between the phase composition of ceramics and strength properties. The choice of (1− x)ZrO2 − xCeO2 composite ceramics as objects of study is due to the great prospects for using them as the basis for inert matrix materials for nuclear dispersed fuel, which can replace traditional uranium fuel in high-temperature nuclear reactors. Using X-ray diffraction, it was found that the variation of the oxide components leads to phase transformations of the Monoclinic-ZrO2 → Monoclinic − Zr0.98Ce0.02O2/Tetragonal − ZrO2 → Tetragonal − Zr0.85Ce0.15O2 → Tetragonal − ZrCeO4/Ce0.1Zr0.9O2 type. As a result of mechanical tests, it was found that the formation of tetragonal phases in the structure of ceramics leads to strengthening of ceramics and an increase in crack resistance, which is due not only to an increase in the crystallinity degree, but also to the effect of dislocation hardening associated with a decrease in grain size. It has been established that a change in the phase composition due to phase transformations and displacement of the ZrO2 phase from the ceramic structure with its transformation into the phase of partial replacement of Zr0.85Ce0.15O2 or Ce0.1Zr0.9O2 leads to the strengthening of ceramics by more than 3.5–4 times. The results of resistance to crack formation under single compression showed that the formation of the ZrCeO4 phase in the structure of ceramics leads to an increase in the resistance of ceramics to cracking by more than 2.5 times

Study of Structural and Strength Changes in Lithium-Containing Ceramics—Potential Blanket Materials for Nuclear Power, Subjected to High-Dose Proton Irradiation

The paper considers the hydrogenation processes in Li2TiO3 ceramics under irradiation with protons with an energy of 500 keV and fluences of 1 × 1010–5 × 1017 ion/cm2. The choice of the type of irradiation, as well as the irradiation fluences, is based on the possibilities of modeling hydrogenation processes and studying the kinetics of structural changes caused by the accumulation of radiation damage. The choice of Li2TiO3 ceramics as objects of research is due to their prospects for using as blanket materials of thermonuclear reactors for the tritium production and accumulation. It was found that the formation of point defects and their subsequent evolution associated with the formation of complex compounds and the filling of pores, followed by the formation of gas-filled bubbles, the presence of which leads to a decrease in crack resistance and resistance to destruction of the near-surface layer. Based on the data on structural changes and evolution of the crystal lattice parameters, its swelling, a description of the destruction processes associated with hydrogenation in Li2TiO3 ceramics was proposed. Also, during the studies, it was found that at irradiation fluences above 1 × 1017 ion/cm2, the appearance of impurity inclusions characteristic of the TiO2 phase was observed, the presence of which indicates the crystal lattice destruction processes because of accumulation of radiation damage and deformations caused by them. Critical doses are established at which there is a sharp deterioration in strength and crack resistance, reflecting the resistance of ceramics to mechanical external influences

Study of Radiation Damage Processes Caused by Hydrogen Embrittlement in Lithium Ceramics under High-Temperature Irradiation

The aim of this work is to study the hydrogenation processes in lithium-containing ceramics under high-temperature irradiation. Irradiation was carried out with protons with an energy of 1 MeV and fluences of 1015–1017 ion/cm2 at irradiation temperatures of 300–1000 K. The choice of irradiation conditions is due to the possibility of simulation of the radiation damage accumulation processes in the near-surface layer of Li2TiO3 ceramics, as well as establishing the dependences of changes in structural parameters during temperature heating of samples during irradiation. It has been established that at irradiation fluences of 1015–1016 ion/cm2, the formation of dislocation defects is observed, the density of which has a pronounced dependence on the irradiation temperature. At irradiation fluence above 5 × 1016 ion/cm2, an increase in the crystal structure deformation is observed, due to swelling processes as a result of implanted hydrogen accumulation in the near-surface layer structure. At the same time, an increase in the irradiation temperature leads to a decrease in the swelling value, which is due to the accelerated migration of implanted hydrogen in the near-surface layer and its release through the existing pores. Results of mechanical tests showed that the swelling of the crystal structure and its deformation leads to embrittlement and a partial decrease in the strength of the near-surface layer. The obtained research results will further allow us to evaluate the resistance of lithium ceramics to the processes of hydrogenation and destruction as a result of the formation of gas-filled cavities in the structure of the near-surface layer

Study of Radiation Damage Processes Caused by Hydrogen Embrittlement in Lithium Ceramics under High-Temperature Irradiation

The aim of this work is to study the hydrogenation processes in lithium-containing ceramics under high-temperature irradiation. Irradiation was carried out with protons with an energy of 1 MeV and fluences of 1015–1017 ion/cm2 at irradiation temperatures of 300–1000 K. The choice of irradiation conditions is due to the possibility of simulation of the radiation damage accumulation processes in the near-surface layer of Li2TiO3 ceramics, as well as establishing the dependences of changes in structural parameters during temperature heating of samples during irradiation. It has been established that at irradiation fluences of 1015–1016 ion/cm2, the formation of dislocation defects is observed, the density of which has a pronounced dependence on the irradiation temperature. At irradiation fluence above 5 × 1016 ion/cm2, an increase in the crystal structure deformation is observed, due to swelling processes as a result of implanted hydrogen accumulation in the near-surface layer structure. At the same time, an increase in the irradiation temperature leads to a decrease in the swelling value, which is due to the accelerated migration of implanted hydrogen in the near-surface layer and its release through the existing pores. Results of mechanical tests showed that the swelling of the crystal structure and its deformation leads to embrittlement and a partial decrease in the strength of the near-surface layer. The obtained research results will further allow us to evaluate the resistance of lithium ceramics to the processes of hydrogenation and destruction as a result of the formation of gas-filled cavities in the structure of the near-surface layer

The Synthesis, Properties, and Stability of Lithium-Containing Nanostructured Nickel-Doped Ceramics

Lithium-containing ceramics have several great potential uses for tritium production, as well as its accumulation. However, their use is limited due to their poor resistance to external influences, mechanical pressure, and temperature changes. In this work, initial nanostructured ceramic powders were obtained using the sol-gel method, by mixing TiO2 and LiClO4·3H2O with the subsequent addition of NiO nanoparticles to the reaction mixture; these powders were subsequently subjected to thermal annealing at a temperature of 1000 °C for 10 h. Thermal annealing was used to initiate the phase transformation processes, and to remove structural distortions resulting from synthesis. During the study, it was found that the addition of NiO nanoparticles leads to the formation of solid solutions by a type of Li0.94Ni1.04Ti2.67O7 substitution, which leads to an increase in the crystallinity and structural ordering degree. At the same time, the grain sizes of the synthesized ceramics change their shape from rhomboid to spherical. During analysis of the strength characteristics, it was found that the formation of Li0.94Ni1.04Ti2.67O7 in the structure leads to an increase in hardness and crack resistance; this change is associated with dislocation. When analyzing changes in resistance to cracking, it was found that, during the formation of the Li0.94Ni1.04Ti2.67O7 phase in the structure and the subsequent displacement of the Li2TiO3 phase from the composition, the crack resistance increases by 15% and 37%, respectively, which indicates an increase in the resistance of ceramics to cracking and the formation of microcracks under external influences. This hardening and the reinforcing effect are associated with the replacement of lithium ions by nickel ions in the crystal lattice structure

Study of Radiation Resistance of WO3 Microparticles under Irradiation with Heavy Kr15+ and Xe22+ Ions

In this work, we consider the effect of irradiation with heavy Kr15+ and Xe22+ ions on the change in the structural and strength properties of WO3 microparticles, which are among the candidates for inert matrix materials. Irradiation with heavy Kr15+ and Xe22+ ions was chosen to determine the possibility of simulation of radiation damage comparable to the impact of fission fragments. During the studies, it was found that the main changes in the structural properties with an increase in the irradiation fluence are associated with the crystal lattice deformation and its anisotropic distortion, which is most pronounced during irradiation with heavy Kr15+ ions. An assessment of the gaseous swelling effect due to the radiation damage accumulation showed that a change in the ion type during irradiation leads to an increase in the swelling value by more than 8–10%. Results of strength changes showed that the most intense decrease in the hardness of the near-surface layer is observed when the fluence reaches more than 1012 ion/cm2, which is typical for the effect of overlapping radiation damage in the material. The dependences obtained for the change in structural and strength properties can later be used to evaluate the effectiveness of the use of refractory oxide materials for their use in the creation of inert matrices of nuclear fuel

Ion-Track Template Synthesis and Characterization of ZnSeO3 Nanocrystals

A.I.P. thanks the Institute of Solid-State Physics, University of Latvia. ISSP UL as the Center of Excellence is supported through the Framework Program for European universities. The work was carried out within the framework of the grant AP05134367 of the Ministry Funding: The work was carried out within the framework of the grant AP05134367 of the Ministry of education and Science Science of of the Republic Republic of Kazakhstan.ZnSeO3 nanocrystals with an orthorhombic structure were synthesized by electrochemical and chemical deposition into SiO2/Si ion-track template formed by 200 MeV Xe ion irradiation with the fluence of 107 ions/cm2 . The lattice parameters determined by the X-ray diffraction and calculated by the CRYSTAL computer program package are very close to each other. It was found that ZnSeO3 has a direct band gap of 3.8 eV at the Γ-point. The photoluminescence excited by photons at 300 nm has a low intensity, arising mainly due to zinc and oxygen vacancies. Photoluminescence excited by photons with a wavelength of 300 nm has a very low intensity, presumably due to electronic transitions of zinc and oxygen vacancies. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART2

Study of Phase Formation Processes in Li2ZrO3 Ceramics Obtained by Mechanochemical Synthesis

The article is dedicated to the study of the phase formation processes in Li2ZrO3 ceramics obtained by the method of solid phase synthesis. Interest in these types of ceramics is due to their great potential for use as blanket materials in thermonuclear reactors, as well as being one of the candidates for tritium breeder materials. Analysis of the morphological features of the synthesized ceramics depending on the annealing temperature showed that the average grain size is 90–110 nm; meanwhile the degree of homogeneity is more than 90% according to electronic image data processing results. The temperature dependences of changes in the structural and conducting characteristics, as well as the phase transformation dynamics, have been established. It has been determined that a change in the phase composition by displacing the impurity LiO and ZrO2 phases results in the compaction of ceramics, as well as a decrease in their porosity. These structural changes are due to the displacement of LiO and ZrO2 impurity phases from the ceramic structure and their transformation into the Li2ZrO3 phase. During research, the following phase transformations that directly depend on the annealing temperature were established: LiO/ZrO2/Li2ZrO3 → LiO/Li2ZrO3 → Li2ZrO3. During analysis of the obtained current-voltage characteristics, depending on the annealing temperature, it was discovered that the formation of the Li2ZrO3 ordered phase in the structure results in a rise in resistance by three orders of magnitude, which indicates the dielectric nature of the ceramics